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Asymmetric diels - alder reacrions with α-chloronitroso compounds- II. The use of a carbohydrate derived α-chloro-α-nitroso ether

✍ Scribed by H. Felber; G Kresze; H. Braun; A. Vasella


Publisher
Elsevier Science
Year
1984
Tongue
French
Weight
118 KB
Volume
25
Category
Article
ISSN
0040-4039

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✦ Synopsis


The Diels-Alder reaction of 1,3-cyclohexadiene with the a-chloro-a-nitroso ether 2, prepared from mannose via the lactone oxime 1, gives the adduct 3 with l-(S),4-(R) configuration in 69 % chemical yield and z 95 % enantiome& excess.